Canonical Allele Identifier: PA2579978814
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.His424Tyr
CA367397245
NM_000162.5:c.1270C>T